Evidence map›Paper›PMID 27050036›Full record

ArticleBiodemography and social biology2016

Differential Vulnerability to Early-Life Parental Death: The Moderating Effects of Family Suicide History on Risks for Major Depression and Substance Abuse in Later Life.

Michael S Hollingshaus, Hilary Coon, Sheila E Crowell, Douglas D Gray, Heidi A Hanson, Richard Pimentel, Ken R Smith

Open access · greenAbstract read
In one paragraph

Article in Biodemography and social biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.2field-weighted citation impact, top 20% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 8 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Michael S Hollingshausa Department of Sociology , University of Utah , Salt Lake City , UT , USA.
Hilary Coonb Department of Psychiatry , University of Utah , Salt Lake City , UT , USA.
Sheila E Crowellc Department of Psychology , University of Utah , Salt Lake City , UT , USA.
Douglas D Grayb Department of Psychiatry , University of Utah , Salt Lake City , UT , USA.
Heidi A Hansond Department of Family and Preventive Medicine , University of Utah , Salt Lake City , UT , USA.
Richard Pimentele Population Sciences , Huntsman Cancer Institute , Salt Lake City , UT , USA.
Ken R Smithf Human Development & Family Studies , University of Utah , Salt Lake City , UT , USA.
University of Utah · USHuntsman Cancer Institute · US

Funding

UTAH REGIONAL CANCER CENTERP30CA042014 · NCI · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Jared P Rutter · 1986 to 2026
$72.6M
The Utah Study of Fertility, Longevity and AgingR01AG022095 · NIA · UNIVERSITY OF UTAH · PI SMITH, KEN R · 2003 to 2015
$9.4M
Genetic analysis of high-risk Utah suicide pedigreesR01MH099134 · NIMH · UNIVERSITY OF UTAH · PI COON, HILARY · 2013 to 2017
$3.9M
NCI NIH HHS P30 CA042014NCI NIH HHS P30 CA42014NIA NIH HHS AG022095NIA NIH HHS R01 AG022095NIMH NIH HHS R01 MH099134
6 · The paper itself

Abstract

Only a portion of those individuals exposed to parental death in early life (PDE) develop behavioral health disorders. We utilized demographic pedigree data from the Utah Population Database to test for differential vulnerability to PDE by creating a risk score of familial susceptibility to suicide (FS) at the population level. Using logistic panel regression models, we tested for multiplicative interactions between PDE and FS on the risks of major depressive disorder (MDD) and substance abuse (SA), measured using Medicare claims, after age 65. The final sample included 155,983 individuals (born 1886-1944), yielding 1,431,060 person-years at risk (1992-2009). Net of several potential confounders, including probability of survival to age 65, we found an FS × PDE interaction for females, in which PDE and FS as main effects had no impact but jointly increased MDD risk. No statistically significant main or interactive effects were found for SA among females or for either phenotype among males. Our findings are consistent with a differential vulnerability model for MDD in females, in which early-life stress increases the risk for poor behavioral health only among the vulnerable. Furthermore, we demonstrate how demographic and pedigree data might serve as tools for investigating differential vulnerability hypotheses.

Indexed as

AdultAgedDatabases, FactualFemaleHumansMajor Depressive DisorderMaleMiddle AgedParental DeathRegression AnalysisSex FactorsStress, PsychologicalSubstance-Related DisordersSuicideSurvival AnalysisUtah

Identifiers

PMID27050036
PMCPMC4929083
OpenAlexW2332136606

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.